Huang Yu-Shan, Sun Hsin-Yun, Ho Shu-Yuan, Lin Kuan-Yin, Liu Wang-Da, Sheng Wang-Huei, Hsieh Szu-Min, Chuang Yu-Chung, Su Li-Hsin, Su Yi-Ching, Liu Wen-Chun, Chang Sui-Yuan, Hung Chien-Ching
Department of Internal Medicine, National Taiwan University Hospital and National Taiwan University College of Medicine, Taipei, Taiwan.
Department of Laboratory Medicine, National Taiwan University Hospital and National Taiwan University College of Medicine, Taipei, Taiwan.
Clin Infect Dis. 2025 Jan 2. doi: 10.1093/cid/ciae655.
Tenofovir-containing antiretroviral therapy (ART) improves survival in HBV-coinfected people with HIV (PWH). We investigated the incidence of HDV infection and its clinical impact in HBV-coinfected PWH in the era of tenofovir-containing ART.
Between 2011 and 2022, HBV-coinfected PWH were included and followed until December 2023. Anti-HDV antibody screening was performed using sequentially archived blood samples. The timing of incident HDV infection was estimated as the midpoint between the last time point of anti-HDV-negative samples and the first time point of anti-HDV-positive samples. Differences in survival and liver-related outcomes between HDV-infected and HDV-uninfected PWH were analyzed.
534 HBV-coinfected PWH were included and 36 (6.7%) tested HDV-seropositive at baseline. During 3987.78 person-years of follow-up (PYFU), 50 (10.0%) of 498 anti-HDV-negative PWH seroconverted for HDV, with an overall incidence rate of 12.54 per 1000 PYFU. 88.0% (44/50) of HDV seroconverters were men who have sex with men. After a median follow-up of 10.2 years (84.7% of the follow-up period covered by tenofovir-containing ART), the all-cause mortality was 4.7% (25/534). HDV-infected PWH had significantly higher rates of liver-related mortality (3.5% vs 0.4%, P=.032), cirrhosis (11.3% vs 3.6%, P=.008), and hepatitis flare (28.2% vs 14.2%, P=.001) than HDV-uninfected PWH. In multivariate Cox analysis, HDV infection was associated with liver-related mortality (adjusted HR, 9.696; 95% CI, 1.284-73.222, P=.028). The risk of hepatocellular carcinoma was similar for HDV-infected and HDV-uninfected PWH.
HBV-coinfected PWH remain at risk for HDV superinfection and HDV infection is associated with liver-related death in the era of tenofovir-containing ART.
含替诺福韦的抗逆转录病毒疗法(ART)可提高合并感染乙肝病毒(HBV)的艾滋病毒感染者(PWH)的生存率。我们调查了在含替诺福韦的ART时代,合并感染HBV的PWH中丁型肝炎病毒(HDV)感染的发生率及其临床影响。
纳入2011年至2022年间合并感染HBV的PWH,并随访至2023年12月。使用序贯存档的血液样本进行抗HDV抗体筛查。将HDV感染发生时间估计为抗HDV阴性样本的最后时间点与抗HDV阳性样本的第一个时间点之间的中点。分析HDV感染组和未感染组PWH在生存率和肝脏相关结局方面的差异。
纳入534例合并感染HBV的PWH,36例(6.7%)在基线时HDV血清学检测呈阳性。在3987.78人年的随访期(PYFU)内,498例抗HDV阴性的PWH中有50例(10.0%)发生HDV血清学转换,总发病率为每1000 PYFU 12.54例。88.0%(44/50)的HDV血清学转换者为男男性行为者。在中位随访10.2年(含替诺福韦的ART覆盖随访期的84.7%)后,全因死亡率为4.7%(25/534)。与未感染HDV的PWH相比,感染HDV的PWH肝脏相关死亡率(3.5%对0.4%,P=0.032)、肝硬化(11.3%对3.6%,P=0.008)和肝炎发作(28.2%对14.2%,P=0.001)的发生率显著更高。在多变量Cox分析中,HDV感染与肝脏相关死亡率相关(调整后HR,9.696;95%CI,1.284-73.222,P=0.028)。HDV感染组和未感染组PWH发生肝细胞癌的风险相似。
合并感染HBV的PWH仍有HDV重叠感染风险,在含替诺福韦的ART时代,HDV感染与肝脏相关死亡有关。